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  5. NDC Package Code: 49726-043-60 Activive

NDC Package 49726-043-60 Activive

Alfalfa,Ambra Grisea,Anacardium Orientale,Argentum Nitricum,Aurum Metallicum,Avena - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
49726-043-60
Package Description:
60 TABLET in 1 BOTTLE, PLASTIC
Product Code:
49726-043
Proprietary Name:
Activive
Non-Proprietary Name:
Alfalfa, Ambra Grisea, Anacardium Orientale, Argentum Nitricum, Aurum Metallicum, Avena Sativa, Caladium Seguinum, Calcarea Carbonica, Cocculus Indicus, Gelsemium Sempervirens, Ignatia Amara, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Nux Moschata, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Sepia, Silicea, Sulphur
Substance Name:
Alfalfa; Ambergris; Anamirta Cocculus Seed; Avena Sativa Flowering Top; Dibasic Potassium Phosphate; Dieffenbachia Seguine; Gelsemium Sempervirens Root; Gold; Lycopodium Clavatum Spore; Nutmeg; Oyster Shell Calcium Carbonate, Crude; Phosphoric Acid; Phosphorus; Selenium; Semecarpus Anacardium Juice; Sepia Officinalis Juice; Silicon Dioxide; Silver Nitrate; Sodium Chloride; Strychnos Ignatii Seed; Sulfur
Usage Information:
For the temporary relief of symptoms such as:• exhaustion• dullness• drowsiness• muscle weaknessProduct indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA. For the temporary relief of symptoms such as:• exhaustion• dullness• drowsiness• muscle weaknessProduct indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.
11-Digit NDC Billing Format:
49726004360
Product Type:
Human Otc Drug
Labeler Name:
Hellolife, Inc.
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ALFALFA 10 [hp_X]/1
  • AMBERGRIS 10 [hp_X]/1
  • ANAMIRTA COCCULUS SEED 10 [hp_X]/1
  • AVENA SATIVA FLOWERING TOP 10 [hp_X]/1
  • DIBASIC POTASSIUM PHOSPHATE 10 [hp_X]/1
  • DIEFFENBACHIA SEGUINE 10 [hp_X]/1
  • GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/1
  • GOLD 10 [hp_X]/1
  • LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/1
  • NUTMEG 10 [hp_X]/1
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/1
  • PHOSPHORIC ACID 10 [hp_X]/1
  • PHOSPHORUS 10 [hp_X]/1
  • SELENIUM 10 [hp_X]/1
  • SEMECARPUS ANACARDIUM JUICE 10 [hp_X]/1
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/1
  • SILICON DIOXIDE 10 [hp_X]/1
  • SILVER NITRATE 10 [hp_X]/1
  • SODIUM CHLORIDE 10 [hp_X]/1
  • STRYCHNOS IGNATII SEED 10 [hp_X]/1
  • SULFUR 10 [hp_X]/1
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Food Additives - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-19-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49726-043-60?

    The NDC Packaged Code 49726-043-60 is assigned to a package of 60 tablet in 1 bottle, plastic of Activive, a human over the counter drug labeled by Hellolife, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 49726-043 included in the NDC Directory?

    Yes, Activive with product code 49726-043 is active and included in the NDC Directory. The product was first marketed by Hellolife, Inc. on October 19, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49726-043-60?

    The 11-digit format is 49726004360. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-249726-043-605-4-249726-0043-60